Hello and Welcome! I am very pleased to have you around.
The above repository contains various workflows by which we could be able to perform Human variant calling analysis on sequence data.
The workflows will be implemented with the three most common workflow systems:
For the data, we shall be using the dataset provided by H3ABioNet which can be found here.
Contributions for the project are welcomed. Please fork the repository make your changes then submit a PR.
This project is distributed under the MIT Licence.